Canonical Allele Identifier: PA2826317899
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 558460
ClinVar RCV Id: RCV000674734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ala763Pro
CA250085276
NM_001243182.2:c.2287G>C