Canonical Allele Identifier: PA2825296011
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2453262
ClinVar RCV Id: RCV003182717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg1323Gly
CA362689362
NM_001008844.3:c.3967A>G