Canonical Allele Identifier: PA2829902484
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 362475
ClinVar RCV Id: RCV000275606 RCV000388519 RCV001258244 RCV002523654
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060881.2:p.Pro1102Arg
CA4661767
NM_018411.4:c.3305C>G