Canonical Allele Identifier: PA2499280563
Gene: SATB2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056080.1:p.Asn355Thr
CA350387376
NM_015265.3:c.1064A>C