Canonical Allele Identifier: PA2580524497
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1754908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Leu223Gln
CA269293279
NM_152594.3:c.668T>A