Canonical Allele Identifier: PA2825279526
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3069918
ClinVar RCV Id: RCV004009950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asn590Ile
CA388030786
NM_001005918.3:c.1769A>T