Canonical Allele Identifier: PA100206
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 7340
ClinVar RCV Id: RCV000007765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005135.2:p.Asp1012Asn
CA210694
NM_005144.5:c.3034G>A