Canonical Allele Identifier: PA645426982
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429870
ClinVar RCV Id: RCV000493530 RCV002420259 RCV000819475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Val336Ile
CA7470219
NM_152594.3:c.1006G>A