Allele Registry

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Canonical Allele Identifier: PA2827013898

Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422850

ClinVar RCV Id: RCV000487076 RCV001037910 RCV002455934

ClinVar Variation Id: 535905

ClinVar RCV Id: RCV000644131

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Val686Leu	CA16620093 NM_001318831.2:c.2056G>C CA394279221 NM_001318831.2:c.2056G>T