Canonical Allele Identifier: PA2827327481
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074785
ClinVar RCV Id: RCV004014319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Arg1333Trp
CA250071636
NM_001330578.2:c.3997C>T