Canonical Allele Identifier: PA645503292
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362526
ClinVar RCV Id: RCV000323657 RCV000373623 RCV000961860 RCV004555572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005135.2:p.Arg324Trp
CA4662595
NM_005144.5:c.970C>T