Canonical Allele Identifier: PA2827015138
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro1145Ser
CA16607165
NM_001318831.2:c.3433C>T