Canonical Allele Identifier: PA645478589
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418164
ClinVar RCV Id: RCV000485589 RCV002221154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Ser357Phe
CA16620726
NM_001005361.3:c.1070C>T