Canonical Allele Identifier: PA112593
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7287
ClinVar RCV Id: RCV000007710 RCV000203266 RCV000369987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Gly358Arg
CA248603
NM_001005360.3:c.1072G>A
CA404047977
NM_001005360.3:c.1072G>C