Canonical Allele Identifier: PA916022172
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 462154
ClinVar RCV Id: RCV000525978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Gly72Ala
CA378921260
NM_001318054.2:c.215G>C