Canonical Allele Identifier: PA1139697708
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 962033
ClinVar RCV Id: RCV001235818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala476Val
CA388035654
NM_001330579.2:c.1427C>T