Canonical Allele Identifier: PA2827029708
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_001305963.1:p.Gln2205Glu
CA362694110
NM_001319034.2:c.6613C>G