Canonical Allele Identifier: PA2827326861
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157952
ClinVar RCV Id: RCV000145277 RCV000667056 RCV001576695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala1105Gly
CA171321
NM_001330578.2:c.3314C>G