Canonical Allele Identifier: PA2825297197
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 922332
ClinVar RCV Id: RCV001182364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser2238Thr
CA362695280
NM_001008844.3:c.6712T>A