Canonical Allele Identifier: PA2827028521
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3070119
ClinVar RCV Id: RCV004010151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu1249Pro
CA362684768
NM_001319034.2:c.3746T>C