Canonical Allele Identifier: PA254141
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Ser619Trp
CA254140
NM_001005361.3:c.1856C>G