Canonical Allele Identifier: PA645432303
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala675Thr
CA10583300
NM_000548.5:c.2023G>A