Canonical Allele Identifier: PA2828091606
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486600
ClinVar RCV Id: RCV000570537 RCV001369719 RCV003459405
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ile610Val
CA394273002
NM_001363528.2:c.1828A>G