Canonical Allele Identifier: PA2825295822
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1732187
ClinVar RCV Id: RCV002459243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile1171Met
CA362684235
NM_001008844.3:c.3513T>G