Canonical Allele Identifier: PA2499280550
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001127
ClinVar RCV Id: RCV001297369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056080.1:p.Ala32Thr
CA350388499
NM_015265.3:c.94G>A