Canonical Allele Identifier: PA204993
Gene: DYNC1H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 209107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001367.2:p.Arg309His
CA204992
NM_001376.5:c.926G>A