Canonical Allele Identifier: PA2825296119
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920189
ClinVar RCV Id: RCV001178771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser1407Tyr
CA362689913
NM_001008844.3:c.4220C>A