Canonical Allele Identifier: PA2827027366
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1780468
ClinVar RCV Id: RCV002410061 RCV003774509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu354Pro
CA362675504
NM_001319034.2:c.1061T>C