Canonical Allele Identifier: PA2825296886
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1347740
ClinVar RCV Id: RCV002050667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Gln2049Glu
CA362694110
NM_001008844.3:c.6145C>G