Canonical Allele Identifier: PA915997189
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 465285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Gly786Cys
CA404043779
NM_001190716.1:c.2356G>T