Canonical Allele Identifier: PA915955600
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 647202
ClinVar RCV Id: RCV000801656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala887Thr
CA6988941
NM_000053.4:c.2659G>A