Canonical Allele Identifier: PA303971
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199941
ClinVar RCV Id: RCV000181390 RCV000791642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Val2737Ala
CA007431
NM_004415.4:c.8210T>C