Canonical Allele Identifier: PA091962
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 553828
ClinVar RCV Id: RCV000669351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Pro992His
CA388032212
NM_000053.4:c.2975C>A