Canonical Allele Identifier: PA2827028880
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2117623
ClinVar RCV Id: RCV003027837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1515Asp
CA362689601
NM_001319034.2:c.4545G>C
CA362689602
NM_001319034.2:c.4545G>T