This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2580485184
Gene: ZNF496 HGNC NCBI
ClinVar RCV:
RCV004149950
ClinVar Variation:
2300082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116141.1:p.Glu498Gln
CA40694478
NM_032752.3:c.1492G>C