Canonical Allele Identifier: PA2825296885
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1761306
ClinVar RCV Id: RCV002416810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Gly2048Ser
CA362694103
NM_001008844.3:c.6142G>A