Canonical Allele Identifier: PA162618
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135386
ClinVar RCV Id: RCV000122232 RCV000564577 RCV000644340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1369Gln
CA019956
NM_000548.5:c.4106G>A