Canonical Allele Identifier: PA2825279705
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2139980
ClinVar RCV Id: RCV003066731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asn730Ser
CA6988939
NM_001005918.3:c.2189A>G