Canonical Allele Identifier: PA2827029930
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 178962
ClinVar RCV Id: RCV000155738 RCV001159059 RCV001160404 RCV001160405 RCV001319008 RCV002433682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2349Thr
CA007514
NM_001319034.2:c.7045T>A