Canonical Allele Identifier: PA915989000
Gene: ZMYND10 HGNC NCBI

Linked Data

ClinVar Variation Id: 646133
ClinVar RCV Id: RCV000800360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056980.2:p.Ala184Val
CA352942190
NM_015896.4:c.551C>T