Canonical Allele Identifier: PA2827010440
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2151949
ClinVar RCV Id: RCV003079033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile1632Met
CA394314649
NM_001318829.2:c.4896C>G