Canonical Allele Identifier: PA172115
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Pro627Arg
CA172114
NM_001005361.3:c.1880C>G