Canonical Allele Identifier: PA916066300
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362490
ClinVar RCV Id: RCV000294513 RCV000351806 RCV002523662 RCV002523661
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060881.2:p.Arg856Trp
CA4662081
NM_018411.4:c.2566C>T