Canonical Allele Identifier: PA172102
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158514
ClinVar RCV Id: RCV000145903 RCV000275646 RCV000552861 RCV000679888 RCV002252002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Arg522His
CA172101
NM_001005361.3:c.1565G>A