Canonical Allele Identifier: PA2826935467
Gene: ZMYND10 HGNC NCBI

Linked Data

ClinVar Variation Id: 66021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295308.1:p.Val16Gly
CA214439
NM_001308379.2:c.47T>G