Canonical Allele Identifier: PA2825438834
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile1478Val
CA10583336
NM_001077183.3:c.4432A>G