Canonical Allele Identifier: PA2825572979
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41724
ClinVar RCV Id: RCV000034641 RCV000055595 RCV000122202 RCV000163628 RCV000230505 RCV000714826
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala357Val
CA013675
NM_001114382.3:c.1070C>T