Canonical Allele Identifier: PA2825435150
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 453076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gln371Arg
CA394318377
NM_001077183.3:c.1112A>G