Canonical Allele Identifier: PA2825279514
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2141850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ala576Val
CA6989239
NM_001005918.3:c.1727C>T