Canonical Allele Identifier: PA2827179937
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 450138
ClinVar RCV Id: RCV000522074 RCV001490971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309869.1:p.Val446Met
CA3969726
NM_001322940.2:c.1336G>A