Canonical Allele Identifier: PA2825438344
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2827102
ClinVar RCV Id: RCV003628133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser1344Arg
CA394300235
NM_001077183.3:c.4030A>C
CA394300264
NM_001077183.3:c.4032C>A
CA394300268
NM_001077183.3:c.4032C>G