Canonical Allele Identifier: PA2829980992
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 388436
ClinVar RCV Id: RCV000441035 RCV001086097 RCV001119330 RCV002328977
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1398Ser
CA16607171
NM_021055.3:c.4192C>T