Canonical Allele Identifier: PA2828527996
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 2145164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361451.1:p.Gln57His
CA365534208
NM_001374522.1:c.171G>C
CA365534209
NM_001374522.1:c.171G>T