Canonical Allele Identifier: PA091915
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly943Ser
CA252894
NM_000053.4:c.2827G>A