Canonical Allele Identifier: PA2825296867
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1163847
ClinVar RCV Id: RCV001509263 RCV001865957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile2038Val
CA362694042
NM_001008844.3:c.6112A>G