Canonical Allele Identifier: PA2825692514
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1376888
ClinVar RCV Id: RCV001888222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ser177Asn
CA378921010
NM_001130442.3:c.530G>A