Canonical Allele Identifier: PA2825296288
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_001008844.1:p.Gly1534Ser
CA006920
NM_001008844.3:c.4600G>A