Canonical Allele Identifier: PA2827028971
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1055673
ClinVar RCV Id: RCV001364383 RCV003388004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1587Pro
CA362690053
NM_001319034.2:c.4759T>C