Canonical Allele Identifier: PA2825297126
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 959135
ClinVar RCV Id: RCV001232426 RCV002447162 RCV002491747 RCV004004842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu2203Phe
CA052241
NM_001008844.3:c.6607C>T