Canonical Allele Identifier: PA2827028788
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072930
ClinVar RCV Id: RCV004014944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Lys1449Thr
CA362689159
NM_001319034.2:c.4346A>C