Canonical Allele Identifier: PA2827396428
Gene: ZNF782 HGNC NCBI

Linked Data

ClinVar Variation Id: 2352077
ClinVar RCV Id: RCV004192307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333924.1:p.Ile168Val
CA5142932
NM_001346995.2:c.502A>G