Canonical Allele Identifier: PA2826317509
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 941024
ClinVar RCV Id: RCV001210728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ala465Thr
CA6989240
NM_001243182.2:c.1393G>A