Canonical Allele Identifier: PA092000
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 289465
ClinVar RCV Id: RCV000273499 RCV000665879 RCV001553563 RCV002518085
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr974Met
CA6988862
NM_000053.4:c.2921C>T