Allele Registry

Canonical Allele Identifier: PA2828379609

Gene: ZMYND11 HGNC NCBI

ClinVar RCV:

RCV000413358

ClinVar Variation:

372987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357047.1:p.Pro373Ser	CA16042797 NM_001370118.2:c.1117C>T