Canonical Allele Identifier: PA1139738926
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 949573
ClinVar RCV Id: RCV001221058 RCV003438723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056080.1:p.Met142Ile
CA2046088
NM_015265.3:c.426G>A
CA350389131
NM_015265.3:c.426G>T
CA350389132
NM_015265.3:c.426G>C