Canonical Allele Identifier: PA2827028835
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3075013
ClinVar RCV Id: RCV004015539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr1487_Glu1488del
CA565358152
NM_001319034.2:c.4459_4464del