Canonical Allele Identifier: PA2825296047
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 928561
ClinVar RCV Id: RCV001192667 RCV001524639 RCV004010601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg1346Cys
CA362689512
NM_001008844.3:c.4036C>T