Canonical Allele Identifier: PA2827027318
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 391896
ClinVar RCV Id: RCV000426226 RCV000704787 RCV002379384 RCV003532118 RCV004000565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Val321Leu
CA053369
NM_001319034.2:c.961G>C