Canonical Allele Identifier: PA1139762837
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 961394
ClinVar RCV Id: RCV001235078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser308Thr
CA7470205
NM_152594.3:c.922T>A