Canonical Allele Identifier: PA2825296026
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1749689
ClinVar RCV Id: RCV002359797 RCV003103231 RCV003225233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser1334Cys
CA362689438
NM_001008844.3:c.4001C>G