Canonical Allele Identifier: PA2825294647
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44956
ClinVar RCV Id: RCV000038092 RCV000172533 RCV000249468 RCV001079525 RCV001175837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala261Val
CA007298
NM_001008844.3:c.782C>T