Canonical Allele Identifier: PA2825297227
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1060837
ClinVar RCV Id: RCV001370318 RCV002488159 RCV004006822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser2257Thr
CA052797
NM_001008844.3:c.6769T>A