Canonical Allele Identifier: PA2825436705
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 391969
ClinVar RCV Id: RCV000432659 RCV001015871 RCV001079672 RCV004000567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr849Ala
CA16607307
NM_001077183.3:c.2545A>G