Canonical Allele Identifier: PA2827029682
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2945721
ClinVar RCV Id: RCV003803815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2189Pro
CA362694011
NM_001319034.2:c.6565T>C