Canonical Allele Identifier: PA2579930563
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 964643
ClinVar RCV Id: RCV001238905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala155Val
CA378921211
NM_001130442.3:c.464C>T