Canonical Allele Identifier: PA915997155
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 327987
ClinVar RCV Id: RCV000356221 RCV000537547 RCV000764169 RCV001507414 RCV002429288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.His727Tyr
CA9201542
NM_001190716.1:c.2179C>T