Canonical Allele Identifier: PA2825692505
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 643338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Pro174Ala
CA378921060
NM_001130442.3:c.520C>G