Canonical Allele Identifier: PA2580198918
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2098197
ClinVar RCV Id: RCV003030820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Glu83Asp
CA378921160
NM_001318054.2:c.249G>C
CA378921161
NM_001318054.2:c.249G>T