Canonical Allele Identifier: PA158296
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 133978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Val64Ile
CA158294
NM_001005361.3:c.190G>A