Canonical Allele Identifier: PA1139716247
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 870076
ClinVar RCV Id: RCV001089607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu463Pro
CA362676681
NM_004415.4:c.1388T>C