Canonical Allele Identifier: PA2826318295
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075591
ClinVar RCV Id: RCV004017109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Trp1042Gly
CA388026586
NM_001243182.2:c.3124T>G