Canonical Allele Identifier: PA2826318675
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074785
ClinVar RCV Id: RCV004014319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Arg1300Trp
CA250071636
NM_001243182.2:c.3898C>T