Canonical Allele Identifier: PA916022825
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452351
ClinVar RCV Id: RCV000521882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr979Ser
CA394285482
NM_001318827.2:c.2935A>T
CA394285499
NM_001318827.2:c.2936C>G