Canonical Allele Identifier: PA2826317304
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2157025
ClinVar RCV Id: RCV003077880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ser280Pro
CA6989426
NM_001243182.2:c.838T>C