Canonical Allele Identifier: PA2827009085
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135384
ClinVar Variation Id: 2837265
ClinVar RCV Id: RCV003628312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1206Asp
CA019763
NM_001318829.2:c.3618G>C
CA394297480
NM_001318829.2:c.3618G>T