Canonical Allele Identifier: PA2825280006
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075591
ClinVar RCV Id: RCV004017109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Trp946Gly
CA388026586
NM_001005918.3:c.2836T>G