Canonical Allele Identifier: PA916071700
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gly13Val
CA296055
NM_176795.5:c.38G>T