Canonical Allele Identifier: PA2828114001
Gene: ZNF442 HGNC NCBI

Linked Data

ClinVar Variation Id: 2490208
ClinVar RCV Id: RCV004273828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350703.1:p.Gly248Ala
CA404220702
NM_001363774.2:c.743G>C