Canonical Allele Identifier: PA091886
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1186Ser
CA274098
NM_000053.4:c.3556G>A