ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA204993
Gene: DYNC1H1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
209107
ClinVar RCV Id:
RCV000191045
RCV000236582
RCV001291169
RCV002514093
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001367.2:p.Arg309His
CA204992
NM_001376.5:c.926G>A