Canonical Allele Identifier: PA351808
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222587
ClinVar RCV Id: RCV000208142 RCV000220371 RCV000469566 RCV001185751 RCV001762452 RCV002485359 RCV003298272 RCV003997683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Val2642Ile
CA351806
NM_004415.4:c.7924G>A