Canonical Allele Identifier: PA2580198917
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1713326
ClinVar RCV Id: RCV002302904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Glu83Gln
CA378921166
NM_001318054.2:c.247G>C