Canonical Allele Identifier: PA180889
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Asn86Thr
CA180888
NM_005343.4:c.257A>C