Canonical Allele Identifier: PA2579933191
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2973421
ClinVar RCV Id: RCV003830515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg73Cys
CA216882919
NM_001130442.3:c.217C>T