Canonical Allele Identifier: PA2825295829
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1035484
ClinVar RCV Id: RCV001338360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Val1176Ala
CA362684269
NM_001008844.3:c.3527T>C