Canonical Allele Identifier: PA916022180
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240136
ClinVar RCV Id: RCV000228331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.His87Gln
CA10582922
NM_001318054.2:c.261C>A
CA378921136
NM_001318054.2:c.261C>G