Canonical Allele Identifier: PA2829973160
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406041
ClinVar RCV Id: RCV000470761 RCV001011130 RCV001591076 RCV004000707
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg454Ser
CA029692
NM_021055.3:c.1362G>C
CA394323549
NM_021055.3:c.1362G>T