Allele Registry

Canonical Allele Identifier: PA2827000766

Gene: TSC2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000226468

RCV001550647

RCV002372261

RCV002942108

RCV003317165

RCV003463661

RCV003998844

RCV004532859

ClinVar Variation:

238096

2057881

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.His270Gln	CA10583287 NM_001318827.2:c.810C>G CA394315395 NM_001318827.2:c.810C>A