Canonical Allele Identifier: PA2829600880
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2178513
ClinVar RCV Id: RCV002595577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gly77Asp
CA378924567
NM_005343.4:c.230G>A