Canonical Allele Identifier: PA2829902472
Gene: HR HGNC NCBI

Linked Data

ClinVar Variation Id: 7331
ClinVar RCV Id: RCV000007756
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060881.2:p.Val1081Asp
CA210693
NM_018411.4:c.3242T>A