Canonical Allele Identifier: PA645503333
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362493
ClinVar RCV Id: RCV000306571 RCV000360619 RCV003343797 RCV002523664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005135.2:p.Arg836Leu
CA4662092
NM_005144.5:c.2507G>T