Canonical Allele Identifier: PA2827420102
Gene: ZNF136 HGNC NCBI

Linked Data

ClinVar Variation Id: 161614
ClinVar RCV Id: RCV000149150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334943.1:p.Leu263Val
CA174454
NM_001348014.2:c.787T>G