Canonical Allele Identifier: PA645503356
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362475
ClinVar RCV Id: RCV000275606 RCV000388519 RCV001258244 RCV002523654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005135.2:p.Pro1157Arg
CA4661767
NM_005144.5:c.3470C>G