Canonical Allele Identifier: PA1139670736
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 882966
ClinVar RCV Id: RCV001113063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.His889Arg
CA388034442
NM_000053.4:c.2666A>G