Canonical Allele Identifier: PA2826162763
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060207
ClinVar RCV Id: RCV001369603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Asn363Ser
CA404048008
NM_001190716.1:c.1088A>G