Canonical Allele Identifier: PA658810985
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 507843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Thr313Met
CA7470206
NM_152594.3:c.938C>T