Canonical Allele Identifier: PA2825296871
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3071735
ClinVar RCV Id: RCV004016229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg2040Gly
CA362694056
NM_001008844.3:c.6118C>G