Canonical Allele Identifier: PA2825296052
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 567189
ClinVar RCV Id: RCV000687198 RCV002352121 RCV002493150 RCV004004261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Tyr1348His
CA045899
NM_001008844.3:c.4042T>C