Canonical Allele Identifier: PA2827026818
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2932659
ClinVar RCV Id: RCV003797825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2Thr
CA362675411
NM_001319034.2:c.5G>C