Canonical Allele Identifier: PA2825280355
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074785
ClinVar RCV Id: RCV004014319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Arg1204Trp
CA250071636
NM_001005918.3:c.3610C>T