Canonical Allele Identifier: PA2826977565
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1011612
ClinVar RCV Id: RCV001309436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Val108Ala
CA378920872
NM_001318054.2:c.323T>C