Canonical Allele Identifier: PA2827396439
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_001333924.1:p.Tyr374His
CA5142825
NM_001346995.2:c.1120T>C