Canonical Allele Identifier: PA658677157
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV001291283
ClinVar Variation:
446598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073932.1:p.Thr65Pro
CA382241467
NM_001080463.2:c.193A>C