Canonical Allele Identifier: PA2825296863
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 848435
ClinVar RCV Id: RCV001052193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Gly2037Asp
CA362694038
NM_001008844.3:c.6110G>A