Canonical Allele Identifier: PA2825437039
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 664836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser955Asn
CA043671
NM_001077183.3:c.2864G>A