Canonical Allele Identifier: PA2825436890
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2100443
ClinVar RCV Id: RCV003025893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Phe908Leu
CA394279532
NM_001077183.3:c.2722T>C
CA394279543
NM_001077183.3:c.2724T>G
CA394279545
NM_001077183.3:c.2724T>A