Canonical Allele Identifier: PA2825435897
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala607Val
CA015881
NM_001077183.3:c.1820C>T