Canonical Allele Identifier: PA2827028869
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1750019
ClinVar RCV Id: RCV002353286 RCV003096890 RCV004005706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Tyr1504Cys
CA362689526
NM_001319034.2:c.4511A>G