Canonical Allele Identifier: PA2827326072
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 647202
ClinVar RCV Id: RCV000801656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala809Thr
CA6988941
NM_001330578.2:c.2425G>A