Canonical Allele Identifier: PA915978308
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV001291171
ClinVar Variation:
446584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Leu2192Phe
CA382249012
NM_001377.3:c.6574C>T