Canonical Allele Identifier: PA122546
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12600
ClinVar RCV Id: RCV000013431 RCV000013432 RCV000013433 RCV000032850 RCV000157912 RCV000438340 RCV000428111 RCV003415692 RCV004018622
ClinVar Variation Id: 279921
ClinVar RCV Id: RCV000322736
ClinVar Variation Id: 1209208
ClinVar RCV Id: RCV001577794 RCV001732216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly12Val
CA122545
NM_005343.4:c.35G>T
CA10603217
NM_005343.4:c.35_36delinsTA
CA658795203
NM_005343.4:c.35_36delinsTT
CA2695212980
NM_005343.4:c.35_36delinsTG