Canonical Allele Identifier: PA2825185810
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040960
ClinVar RCV Id: RCV001344698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu1231Pro
CA394292479
NM_000548.5:c.3692T>C