Canonical Allele Identifier: PA2825263945
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Ser357Phe
CA16620726
NM_001005360.3:c.1070C>T