Canonical Allele Identifier: PA178032
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 165293
ClinVar RCV Id: RCV000151932 RCV000340177 RCV001813394 RCV003975184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ile234Met
CA178031
NM_152594.3:c.702C>G