Canonical Allele Identifier: PA2573099390
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1326221
ClinVar RCV Id: RCV001786282 RCV002034619
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Met425Val
CA7470256
NM_152594.3:c.1273A>G