Canonical Allele Identifier: PA2828420947
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1503Ser
CA394304927
NM_001370405.1:c.4507G>T