Canonical Allele Identifier: PA2826318146
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1702720
ClinVar RCV Id: RCV002279038
ClinVar Variation Id: 2124458
ClinVar RCV Id: RCV003057170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Met929Leu
CA388030333
NM_001243182.2:c.2785A>T
CA388030341
NM_001243182.2:c.2785A>C