Canonical Allele Identifier: PA1139719514
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 918840
ClinVar RCV Id: RCV001176673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Tyr2029His
CA362690047
NM_004415.4:c.6085T>C