Canonical Allele Identifier: PA2828414809
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626432
ClinVar RCV Id: RCV003382412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1502Val
CA394304934
NM_001370404.1:c.4505C>T