Canonical Allele Identifier: PA2828095421
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207761
ClinVar RCV Id: RCV000190043 RCV000468026 RCV001023818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ile1688Ser
CA054821
NM_001363528.2:c.5063T>G