Canonical Allele Identifier: PA658677299
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV001291178
ClinVar Variation:
446606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073932.1:p.Thr2371Ile
CA382252169
NM_001080463.2:c.7112C>T