Canonical Allele Identifier: PA658678999
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 450138
ClinVar RCV Id: RCV000522074 RCV001490971
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037484.1:p.Val633Met
CA3969726
NM_013352.4:c.1897G>A