Canonical Allele Identifier: PA2825574870
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Phe897Ser
CA017895
NM_001114382.3:c.2690T>C