Canonical Allele Identifier: PA2827029918
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 919801
ClinVar RCV Id: RCV001178209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2341Pro
CA362694973
NM_001319034.2:c.7021T>C