Canonical Allele Identifier: PA891863188
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 590805
ClinVar RCV Id: RCV000721965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala784Val
CA388020448
NM_000053.4:c.2351C>T