Canonical Allele Identifier: PA2573308919
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1509551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ile46Val
CA378924771
NM_176795.5:c.136A>G