Canonical Allele Identifier: PA2825296855
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 357965
ClinVar RCV Id: RCV000277919 RCV000370195 RCV000777728 RCV002411250 RCV000402482 RCV000521787 RCV001403630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu2029Pro
CA051060
NM_001008844.3:c.6086T>C