Canonical Allele Identifier: PA2825266810
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 60688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Phe379Val
CA144625
NM_001005362.3:c.1135T>G