Canonical Allele Identifier: PA2827020219
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1490Ser
CA394304927
NM_001318832.2:c.4468G>T