Canonical Allele Identifier: PA2826261248
Gene: ZMYND11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2442370
ClinVar RCV Id: RCV003149143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189394.1:p.Ala2Thr
CA375841210
NM_001202465.3:c.4G>A