Canonical Allele Identifier: PA112637
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 60688
ClinVar RCV Id: RCV000054501 RCV003447110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Phe379Val
CA144625
NM_001005360.3:c.1135T>G