Canonical Allele Identifier: PA2826261257
Gene: ZMYND11 HGNC NCBI

Linked Data

ClinVar Variation Id: 431123
ClinVar RCV Id: RCV000496111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189394.1:p.Arg26Trp
CA375841367
NM_001202465.3:c.76C>T