Canonical Allele Identifier: PA112567
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7282
ClinVar RCV Id: RCV000007705 RCV000145898 RCV000554046 RCV000626717 RCV000725988 RCV003914819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Glu368Lys
CA118661
NM_001005360.3:c.1102G>A