Canonical Allele Identifier: PA645426986
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 426704
ClinVar RCV Id: RCV000490007
ClinVar Variation Id: 2173880
ClinVar RCV Id: RCV002584805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Glu373Asp
CA391934203
NM_152594.3:c.1119G>C
CA391934204
NM_152594.3:c.1119G>T