Canonical Allele Identifier: PA238388
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 192116
ClinVar RCV Id: RCV000172537 RCV001191383 RCV002516569 RCV003995676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Glu1345Ala
CA004347
NM_004415.4:c.4034A>C