Canonical Allele Identifier: PA2827029705
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 659905
ClinVar RCV Id: RCV000816993 RCV003532278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr2203Met
CA362694102
NM_001319034.2:c.6608C>T