Canonical Allele Identifier: PA172139
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158529
ClinVar RCV Id: RCV000145921 RCV000756033 RCV000802315 RCV000280887 RCV002512574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Asp320Asn
CA172137
NM_001005361.3:c.958G>A