Canonical Allele Identifier: PA174455
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_003428.1:p.Leu295Val
CA174454
NM_003437.5:c.883T>G