Canonical Allele Identifier: PA2825434713
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asn229Ser
CA394312549
NM_001077183.3:c.686A>G