Canonical Allele Identifier: PA2828413637
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074520
ClinVar RCV Id: RCV004014054
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Trp1164Cys
CA394291543
NM_001370404.1:c.3492G>C
CA394291545
NM_001370404.1:c.3492G>T