Canonical Allele Identifier: PA2828412436
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406060
ClinVar RCV Id: RCV000458103 RCV001015427 RCV001119144 RCV004539938 RCV003477947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser802Gly
CA038952
NM_001370404.1:c.2404A>G