Canonical Allele Identifier: PA172099
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Arg465Trp
CA172098
NM_001005361.3:c.1393C>T