Canonical Allele Identifier: PA2827001264
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237964
ClinVar RCV Id: RCV000231211 RCV000765262 RCV001011245 RCV001589172 RCV003998801
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg421Gln
CA10583294
NM_001318827.2:c.1262G>A