Canonical Allele Identifier: PA091877
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 554311
ClinVar RCV Id: RCV000669922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1089Glu
CA388028869
NM_000053.4:c.3266G>A