Canonical Allele Identifier: PA2580207078
Gene: ZNF782 HGNC NCBI

Linked Data

ClinVar Variation Id: 2259237
ClinVar RCV Id: RCV004121250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333920.1:p.Tyr506His
CA5142825
NM_001346991.2:c.1516T>C