Canonical Allele Identifier: PA339655
Gene: DNM2 HGNC NCBI
ClinVar Allele:
215729
ClinVar RCV:
RCV000203274
ClinVar Variation:
218920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Glu341Lys
CA339654
NM_001005360.3:c.1021G>A