Canonical Allele Identifier: PA2580524505
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447509
ClinVar RCV Id: RCV003176480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ala276Thr
CA391933336
NM_152594.3:c.826G>A