Canonical Allele Identifier: PA2825434410
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Lys125Asn
CA048320
NM_001077183.3:c.375G>C
CA394306751
NM_001077183.3:c.375G>T