Canonical Allele Identifier: PA2741954015
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2848931
ClinVar RCV Id: RCV003742149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056080.1:p.Pro576Ala
CA350384272
NM_015265.3:c.1726C>G