Canonical Allele Identifier: PA142271
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 47965
ClinVar RCV Id: RCV000041238 RCV000586558 RCV001086208 RCV001813367 RCV002399395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Val42Ile
CA142270
NM_152594.3:c.124G>A