Canonical Allele Identifier: PA2829600896
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1895526
ClinVar RCV Id: RCV002571664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ile84Val
CA378924480
NM_005343.4:c.250A>G