Canonical Allele Identifier: PA2829600768
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2747523
ClinVar RCV Id: RCV003514885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Val44Ala
CA378924780
NM_005343.4:c.131T>C