Canonical Allele Identifier: PA645478596
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 327980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Thr462Ala
CA9201134
NM_001005361.3:c.1384A>G