Canonical Allele Identifier: PA156162
Gene: ZNF674 HGNC NCBI

Linked Data

ClinVar Variation Id: 130844
ClinVar RCV Id: RCV000118960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034980.1:p.Ile406Thr
CA156161
NM_001039891.2:c.1217T>C