Canonical Allele Identifier: PA2825267174
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 327987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.His723Tyr
CA9201542
NM_001005362.3:c.2167C>T