Canonical Allele Identifier: PA891858000
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 572493
ClinVar RCV Id: RCV000693885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Glu1923Gln
CA362689370
NM_004415.4:c.5767G>C