Canonical Allele Identifier: PA2825438561
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1407Gly
CA051088
NM_001077183.3:c.4219A>G