Canonical Allele Identifier: PA2826999988
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 824096
ClinVar RCV Id: RCV001020923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys12Asn
CA394300828
NM_001318827.2:c.36G>C
CA394300841
NM_001318827.2:c.36G>T