Canonical Allele Identifier: PA913199105
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312398
ClinVar RCV Id: RCV000259729 RCV000755836 RCV000779819 RCV002520888
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ile224Phe
CA6989518
NM_001005918.3:c.670A>T