Canonical Allele Identifier: PA2825692535
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2700340
ClinVar RCV Id: RCV003515374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly180Arg
CA378920980
NM_001130442.3:c.538G>C