Canonical Allele Identifier: PA2827329276
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 100803
ClinVar RCV Id: RCV000087161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly807Ala
CA228984
NM_001330579.2:c.2420G>C