Canonical Allele Identifier: PA645503338
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362490
ClinVar RCV Id: RCV000294513 RCV000351806 RCV002523662 RCV002523661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005135.2:p.Arg856Trp
CA4662081
NM_005144.5:c.2566C>T