Canonical Allele Identifier: PA2825435961
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala623Val
CA16608037
NM_001077183.3:c.1868C>T