Canonical Allele Identifier: PA2827029706
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_001305963.1:p.Gly2204Ser
CA362694103
NM_001319034.2:c.6610G>A