Canonical Allele Identifier: PA2825296570
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 246672
ClinVar RCV Id: RCV000235829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala1792Val
CA10584683
NM_001008844.3:c.5375C>T