Canonical Allele Identifier: PA2825279821
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075599
ClinVar RCV Id: RCV004017117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Met810Thr
CA250082011
NM_001005918.3:c.2429T>C