Canonical Allele Identifier: PA916023359
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65196
ClinVar RCV Id: RCV000055413 RCV000539242 RCV001355778 RCV000765261
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu356Phe
CA013622
NM_001318832.2:c.1066C>T