Canonical Allele Identifier: PA2579931494
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1034833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Glu162Lys
CA378921167
NM_001130442.3:c.484G>A