Canonical Allele Identifier: PA2827028920
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 191641
ClinVar RCV Id: RCV000171918 RCV001204085 RCV003995668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asp1549Glu
CA006670
NM_001319034.2:c.4647C>A
CA362689823
NM_001319034.2:c.4647C>G