Canonical Allele Identifier: PA2827014603
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626434
ClinVar RCV Id: RCV003382414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asp978Glu
CA394292130
NM_001318831.2:c.2934C>A
CA394292131
NM_001318831.2:c.2934C>G