Canonical Allele Identifier: PA2827016096
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238071
ClinVar RCV Id: RCV000228578 RCV000761036 RCV001023346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Phe1413Tyr
CA10583340
NM_001318831.2:c.4238T>A