Canonical Allele Identifier: PA2825279291
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 210480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ile377Val
CA208433
NM_001005918.3:c.1129A>G