Canonical Allele Identifier: PA1139670832
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 928742
ClinVar RCV Id: RCV001193091 RCV001833741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1213Ser
CA6988617
NM_000053.4:c.3637G>A