Canonical Allele Identifier: PA916066292
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362493
ClinVar RCV Id: RCV000306571 RCV000360619 RCV003343797 RCV002523664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060881.2:p.Arg836Leu
CA4662092
NM_018411.4:c.2507G>T