Canonical Allele Identifier: PA2827028829
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1445442
ClinVar RCV Id: RCV001958261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1479Lys
CA362689364
NM_001319034.2:c.4436G>A