Canonical Allele Identifier: PA237128
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 191640
ClinVar RCV Id: RCV000171917 RCV001788057 RCV002478548 RCV002515256 RCV003995667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gln1672Glu
CA004241
NM_004415.4:c.5014C>G