Canonical Allele Identifier: PA2829600689
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1400061
ClinVar RCV Id: RCV001917995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr2Arg
CA378926314
NM_005343.4:c.5C>G