Canonical Allele Identifier: PA891848990
Gene: DYNC1H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 590055
ClinVar RCV Id: RCV000810070 RCV001772019 RCV002318237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001367.2:p.Ala763Val
CA391022660
NM_001376.5:c.2288C>T