Canonical Allele Identifier: PA2827029702
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923617
ClinVar RCV Id: RCV001184444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2201Thr
CA362694087
NM_001319034.2:c.6602G>C