Canonical Allele Identifier: PA658664727
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453028
ClinVar RCV Id: RCV000521434 RCV001836835 RCV003159694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Gly434Val
CA7470261
NM_152594.3:c.1301G>T