Canonical Allele Identifier: PA2573207591
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV001906775
ClinVar Variation:
1405958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368.2:p.Phe116Ser
CA227398265
NM_001377.3:c.347T>C