Canonical Allele Identifier: PA2580524509
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1998564
ClinVar RCV Id: RCV002810546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Lys301Thr
CA391933508
NM_152594.3:c.902A>C