Canonical Allele Identifier: PA2825435125
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile365Val
CA028137
NM_001077183.3:c.1093A>G