Canonical Allele Identifier: PA891866308
Gene: ZNF112 HGNC NCBI

Linked Data

ClinVar Variation Id: 91928
ClinVar RCV Id: RCV000122485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335210.1:p.Ile480Val
CA232179
NM_001348281.2:c.1438A>G