Canonical Allele Identifier: PA2827329196
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 377538
ClinVar RCV Id: RCV000430661 RCV000667536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile773Thr
CA16606473
NM_001330579.2:c.2318T>C