Canonical Allele Identifier: PA2580524511
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765931
ClinVar RCV Id: RCV002378760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Pro305Thr
CA391933532
NM_152594.3:c.913C>A