Canonical Allele Identifier: PA658810970
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 536689
ClinVar RCV Id: RCV000645297 RCV001813535 RCV002360595 RCV003953153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Val212Ile
CA7470143
NM_152594.3:c.634G>A