Canonical Allele Identifier: PA277878
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 44910
ClinVar RCV Id: RCV000038045 RCV000202877 RCV000619831 RCV000770246 RCV000845533 RCV000852995 RCV001080732 RCV003952433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1497Trp
CA004497
NM_004415.4:c.4489C>T