Canonical Allele Identifier: PA2579931371
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2164941
ClinVar RCV Id: RCV003082358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly60Arg
CA378924680
NM_001130442.3:c.178G>C