Canonical Allele Identifier: PA916006173
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 430725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ile991Thr
CA6988743
NM_001243182.2:c.2972T>C