Canonical Allele Identifier: PA658676101
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 462149
ClinVar RCV Id: RCV000546898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu62_Arg68dup
CA658656102
NM_005343.4:c.186_206dup