Canonical Allele Identifier: PA207709
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 210854
ClinVar RCV Id: RCV000193911 RCV000766852 RCV002415823 RCV003507263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Asn658Ser
CA207708
NM_001005360.3:c.1973A>G