Canonical Allele Identifier: PA112485
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 465283
ClinVar RCV Id: RCV000534336 RCV001729629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Ala618Asp
CA404041082
NM_001005360.3:c.1853C>A