Canonical Allele Identifier: PA112602
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Gly537Cys
CA118664
NM_001005360.3:c.1609G>T