Canonical Allele Identifier: PA645480592
Gene: DYNC2H1 HGNC NCBI
ClinVar RCV:
RCV000256416
ClinVar Variation:
266101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073932.1:p.Leu1213Arg
CA10588967
NM_001080463.2:c.3638T>G