Canonical Allele Identifier: PA2827029594
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1760093
ClinVar RCV Id: RCV002400469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Met2117Val
CA050425
NM_001319034.2:c.6349A>G