Canonical Allele Identifier: PA2825297098
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2935108
ClinVar RCV Id: RCV003790762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Tyr2186Cys
CA052095
NM_001008844.3:c.6557A>G