Canonical Allele Identifier: PA916028334
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 439427
ClinVar RCV Id: RCV000507116 RCV000945359 RCV003480658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Asp118Asn
CA6989579
NM_001330579.2:c.352G>A