Canonical Allele Identifier: PA2827027229
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1026944
ClinVar RCV Id: RCV001327474 RCV002412049 RCV003994269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ala261Thr
CA133954649
NM_001319034.2:c.781G>A