Canonical Allele Identifier: PA198751
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2953604
ClinVar RCV Id: RCV003812827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1045Pro
CA005742
NM_004415.4:c.3134G>C