Canonical Allele Identifier: PA2826318389
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35725
ClinVar RCV Id: RCV000029374 RCV000413521
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr1109Met
CA260145
NM_001243182.2:c.3326C>T