Canonical Allele Identifier: PA2827029539
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1402267
ClinVar RCV Id: RCV001906351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Tyr2085Asp
CA362693329
NM_001319034.2:c.6253T>G