Canonical Allele Identifier: PA915983469
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 60688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004936.2:p.Phe379Val
CA144625
NM_004945.4:c.1135T>G