Canonical Allele Identifier: PA256493
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12607
ClinVar RCV Id: RCV000013441 RCV000420974 RCV000432069 RCV000427320 RCV000434059 RCV000438623 RCV000444836
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala146Thr
CA256492
NM_005343.4:c.436G>A