Canonical Allele Identifier: PA2827009824
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1431Ser
CA394304927
NM_001318829.2:c.4291G>T