Canonical Allele Identifier: PA2741953986
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2608058
ClinVar RCV Id: RCV003357619 RCV003778029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056080.1:p.Ser294Asn
CA2045990
NM_015265.3:c.881G>A