Canonical Allele Identifier: PA2573304216
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser308Ala
CA7470204
NM_152594.3:c.922T>G