Canonical Allele Identifier: PA2825279887
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 663298
ClinVar RCV Id: RCV000821152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr855Ile
CA6988784
NM_001005918.3:c.2564C>T