Canonical Allele Identifier: PA2829550779
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004936.2:p.Ser615Trp
CA254140
NM_004945.4:c.1844C>G