Canonical Allele Identifier: PA2826075079
Gene: ZNF764 HGNC NCBI

Linked Data

ClinVar Variation Id: 3198166
ClinVar RCV Id: RCV004492554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166150.1:p.Arg237Trp
CA8007926
NM_001172679.2:c.709C>T