Canonical Allele Identifier: PA303913
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199901
ClinVar RCV Id: RCV000181340 RCV000766888 RCV002354472 RCV002485191 RCV000678705 RCV001179588 RCV001227095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2133Ser
CA006920
NM_004415.4:c.6397G>A