Canonical Allele Identifier: PA2825294782
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2951857
ClinVar RCV Id: RCV003812544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu354Arg
CA362675505
NM_001008844.3:c.1061T>G