Canonical Allele Identifier: PA2827028819
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44931
ClinVar RCV Id: RCV000624492 RCV000626866 RCV000766551 RCV001087393 RCV001189716 RCV002345297 RCV003996348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1472His
CA006581
NM_001319034.2:c.4415G>A