Canonical Allele Identifier: PA2825294873
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 565929
ClinVar RCV Id: RCV000685612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg425Leu
CA133956046
NM_001008844.3:c.1274G>T