Canonical Allele Identifier: PA2825233690
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_001001662.1:p.Ile300Val
CA5142932
NM_001001662.3:c.898A>G