Canonical Allele Identifier: PA645396005
Gene: DYNC1H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 373146
ClinVar RCV Id: RCV000413767
ClinVar Variation Id: 1526100
ClinVar RCV Id: RCV002052120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001367.2:p.Phe623Leu
CA16042868
NM_001376.5:c.1869C>G
CA391019596
NM_001376.5:c.1867T>C
CA391019612
NM_001376.5:c.1869C>A