Canonical Allele Identifier: PA267614
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 120223
ClinVar RCV Id: RCV000106320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu63_Asp69dup
CA267613
NM_005343.4:c.187_207dup