Canonical Allele Identifier: PA915978452
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV000516047
ClinVar Variation:
446617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Gly2649Cys
CA6254356
NM_001377.3:c.7945G>T