Canonical Allele Identifier: PA2826318728
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073899
ClinVar RCV Id: RCV004012441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Asp1335Gly
CA6988416
NM_001243182.2:c.4004A>G