Canonical Allele Identifier: PA2827179442
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 2145164
ClinVar RCV Id: RCV003064889 RCV003250725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309867.1:p.Gln57His
CA365534208
NM_001322938.2:c.171G>C
CA365534209
NM_001322938.2:c.171G>T