Canonical Allele Identifier: PA2827028535
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3224227
ClinVar RCV Id: RCV004518953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu1256Pro
CA362684810
NM_001319034.2:c.3767T>C