Canonical Allele Identifier: PA2825279702
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 100803
ClinVar RCV Id: RCV000087161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly729Ala
CA228984
NM_001005918.3:c.2186G>C