Canonical Allele Identifier: PA658677336
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV001291398
ClinVar Variation:
446548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073932.1:p.Phe2548Ser
CA382254514
NM_001080463.2:c.7643T>C