Canonical Allele Identifier: PA2825435653
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser538Phe
CA10583296
NM_001077183.3:c.1613C>T