Canonical Allele Identifier: PA2580198921
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2416982
ClinVar RCV Id: RCV003111810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ile84Met
CA378921153
NM_001318054.2:c.252C>G