Canonical Allele Identifier: PA645501801
Gene: DNM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 422075
ClinVar RCV Id: RCV000478915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004399.2:p.Tyr390Ser
CA16618755
NM_004408.4:c.1169A>C