Canonical Allele Identifier: PA2825294918
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 520441
ClinVar RCV Id: RCV000624338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Pro453Ser
CA362676552
NM_001008844.3:c.1357C>T