Canonical Allele Identifier: PA2828418880
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49595
ClinVar RCV Id: RCV000042856 RCV000336828
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Phe897Ser
CA017895
NM_001370405.1:c.2690T>C