Canonical Allele Identifier: PA2825267090
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 210854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Asn654Ser
CA207708
NM_001005362.3:c.1961A>G