Canonical Allele Identifier: PA2826162757
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418164
ClinVar RCV Id: RCV000485589 RCV002221154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Ser357Phe
CA16620726
NM_001190716.1:c.1070C>T