Canonical Allele Identifier: PA915955103
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 555617
ClinVar RCV Id: RCV000671472 RCV001805793
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ala990Thr
CA6988627
NM_001005918.3:c.2968G>A