Canonical Allele Identifier: PA2829601162
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1055387
ClinVar RCV Id: RCV001364047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Asn172Ser
CA216881989
NM_005343.4:c.515A>G