Canonical Allele Identifier: PA2827030047
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1763870
ClinVar RCV Id: RCV002414482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Gly2411Arg
CA052774
NM_001319034.2:c.7231G>C
CA362695380
NM_001319034.2:c.7231G>A