Canonical Allele Identifier: PA2825572996
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49140
ClinVar RCV Id: RCV000042395 RCV000413741 RCV001065226
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu362Pro
CA013704
NM_001114382.3:c.1085T>C