Canonical Allele Identifier: PA162596
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135372
ClinVar RCV Id: RCV000122208 RCV000464888 RCV000561143 RCV001086928 RCV003997361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala607Val
CA015881
NM_000548.5:c.1820C>T