Canonical Allele Identifier: PA658677333
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 465283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Ala618Asp
CA404041082
NM_001005361.3:c.1853C>A