Canonical Allele Identifier: PA645478578
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Thr280Met
CA9200897
NM_001005361.3:c.839C>T