Canonical Allele Identifier: PA645478588
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 234708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Val351Met
CA10577588
NM_001005361.3:c.1051G>A