Canonical Allele Identifier: PA658677334
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Ala618Thr
CA404041079
NM_001005361.3:c.1852G>A