Canonical Allele Identifier: PA2828847202
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV000515860
ClinVar Variation:
446564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Leu4269Ser
CA382290910
NM_001377.3:c.12806T>C