Canonical Allele Identifier: PA2827028269
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 357947
ClinVar RCV Id: RCV000272182 RCV000322535 RCV000379457 RCV000485378 RCV000470079 RCV001190426 RCV002480238 RCV002323559 RCV003995896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1049Leu
CA037298
NM_001319034.2:c.3146C>T