Canonical Allele Identifier: PA2499247997
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1035699
ClinVar RCV Id: RCV001338600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Arg90Leu
CA378921116
NM_001318054.2:c.269G>T