Canonical Allele Identifier: PA2825296002
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_001008844.1:p.Arg1316His
CA006581
NM_001008844.3:c.3947G>A