Canonical Allele Identifier: PA2825296035
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 922225
ClinVar RCV Id: RCV001182157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Gln1337Leu
CA362689455
NM_001008844.3:c.4010A>T