Canonical Allele Identifier: PA915978103
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV000516125
ClinVar Variation:
446614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Ile1473Thr
CA382238849
NM_001377.3:c.4418T>C