Canonical Allele Identifier: PA319566
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207769
ClinVar RCV Id: RCV000190052 RCV000227699 RCV001026051 RCV004537600
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro237Leu
CA056182
NM_000548.5:c.710C>T