Canonical Allele Identifier: PA2579930623
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 391700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly60Val
CA16606948
NM_001130442.3:c.179G>T