Canonical Allele Identifier: PA1139717749
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 926590
ClinVar RCV Id: RCV001189270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gln1179Arg
CA362684284
NM_004415.4:c.3536A>G