Canonical Allele Identifier: PA1139719341
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_004406.2:p.Arg1945Cys
CA362689512
NM_004415.4:c.5833C>T