Canonical Allele Identifier: PA2825296019
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3075013
ClinVar RCV Id: RCV004015539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Thr1331_Glu1332del
CA565358152
NM_001008844.3:c.3991_3996del