Canonical Allele Identifier: PA2827028272
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1171750
ClinVar RCV Id: RCV001525094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Cys1052Phe
CA362683143
NM_001319034.2:c.3155G>T