Canonical Allele Identifier: PA2499298964
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022406
ClinVar RCV Id: RCV001322309 RCV004035060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ala406Val
CA7470248
NM_152594.3:c.1217C>T