Canonical Allele Identifier: PA915978105
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV000516112
ClinVar Variation:
446596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Cys1518Tyr
CA382239171
NM_001377.3:c.4553G>A