Canonical Allele Identifier: PA2825296096
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920021
ClinVar RCV Id: RCV001178512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile1387Met
CA046130
NM_001008844.3:c.4161C>G