Canonical Allele Identifier: PA1139699181
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 850426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Arg85Pro
CA5779219
NM_001318054.2:c.254G>C