Canonical Allele Identifier: PA645478581
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 327977
ClinVar RCV Id: RCV000406403 RCV000641109 RCV003144214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Arg297His
CA9200926
NM_001005361.3:c.890G>A