Canonical Allele Identifier: PA2827030067
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 924961
ClinVar RCV Id: RCV001186628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Gly2427Arg
CA362695485
NM_001319034.2:c.7279G>A
CA362695486
NM_001319034.2:c.7279G>C