Canonical Allele Identifier: PA2499247999
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1024818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Pro94Ser
CA378921072
NM_001318054.2:c.280C>T