Canonical Allele Identifier: PA2825437799
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265989
ClinVar RCV Id: RCV000256373 RCV003469206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser1188Phe
CA10588935
NM_001077183.3:c.3563C>T