Canonical Allele Identifier: PA2825266601
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Pro226Leu
CA9200855
NM_001005362.3:c.677C>T