Canonical Allele Identifier: PA2580311538
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1895478
ClinVar RCV Id: RCV002569461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser1894Arg
CA362689172
NM_004415.4:c.5680A>C
CA362689178
NM_004415.4:c.5682T>A
CA362689179
NM_004415.4:c.5682T>G