Canonical Allele Identifier: PA2825267051
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Leu617Pro
CA172112
NM_001005362.3:c.1850T>C