Canonical Allele Identifier: PA916023658
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65184
ClinVar RCV Id: RCV000055401 RCV002513720 RCV003380408
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala618Ser
CA015864
NM_001318832.2:c.1852G>T