Allele Registry

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Canonical Allele Identifier: PA2825439079

Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057471

ClinVar RCV Id: RCV001366460

ClinVar Variation Id: 1360336

ClinVar RCV Id: RCV001904839

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Gln1549His	CA394308160 NM_001077183.3:c.4647A>C CA394308161 NM_001077183.3:c.4647A>T