Canonical Allele Identifier: PA2499233282
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala1546Ser
CA394304927
NM_000548.5:c.4636G>T