Canonical Allele Identifier: PA2827326593
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1018093
ClinVar RCV Id: RCV001317345 RCV001844283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Cys1001Arg
CA388029778
NM_001330578.2:c.3001T>C