Canonical Allele Identifier: PA2825279749
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3064956
ClinVar RCV Id: RCV003990033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr770Lys
CA388032373
NM_001005918.3:c.2309C>A