Canonical Allele Identifier: PA3057522304
Gene: SATB2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056080.1:p.Thr354Ser
CA350387384
NM_015265.3:c.1061C>G
CA350387387
NM_015265.3:c.1060A>T