Canonical Allele Identifier: PA2825297116
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 653551
ClinVar RCV Id: RCV000809341 RCV001182978 RCV003413625 RCV002440739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile2198Thr
CA052174
NM_001008844.3:c.6593T>C