Canonical Allele Identifier: PA2827027019
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 910568
ClinVar RCV Id: RCV001162438 RCV001162437 RCV001162439 RCV001190883 RCV002320382 RCV002032499 RCV002505742 RCV003317437 RCV004000262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg105Gln
CA037337
NM_001319034.2:c.314G>A