Canonical Allele Identifier: PA122550
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12602
ClinVar RCV Id: RCV000013436 RCV000013435 RCV000022796 RCV000029209 RCV000081295 RCV000149828 RCV000417494 RCV000422253 RCV000425542 RCV000430725 RCV000432342 RCV000433576 RCV000432945 RCV000438022 RCV000440297 RCV000443940 RCV000430608 RCV000419709 RCV000420366 RCV000435163 RCV000422656 RCV000423310 RCV000424896 RCV000440863 RCV000440993 RCV000445039 RCV000427772 RCV000430011 RCV000432984 RCV000440237 RCV000487471 RCV001257537 RCV001255689 RCV001813185 RCV003156059 RCV003398496 RCV002453256 RCV003450635 RCV003450636
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Ser
CA122549
NM_005343.4:c.34G>A