Canonical Allele Identifier: PA2827028667
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1737156
ClinVar RCV Id: RCV002359523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1343Ala
CA362685386
NM_001319034.2:c.4028A>C