Canonical Allele Identifier: PA2827330169
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3849
ClinVar RCV Id: RCV000004053 RCV001507825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly1182Arg
CA252890
NM_001330579.2:c.3544G>A
CA388022028
NM_001330579.2:c.3544G>C