Canonical Allele Identifier: PA2825297091
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2002359
ClinVar RCV Id: RCV002820348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Pro2178Leu
CA362694930
NM_001008844.3:c.6533C>T