Canonical Allele Identifier: PA185911
Gene: DYNC1H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001367.2:p.Arg1201Ser
CA185910
NM_001376.5:c.3603G>T
CA391035747
NM_001376.5:c.3603G>C