Canonical Allele Identifier: PA191941
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185434
ClinVar RCV Id: RCV000164859 RCV000407000 RCV001086946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala862Thr
CA017691
NM_000548.5:c.2584G>A