Canonical Allele Identifier: PA2499298965
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046000
ClinVar RCV Id: RCV001350496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Cys433Tyr
CA7470260
NM_152594.3:c.1298G>A