Canonical Allele Identifier: PA2829975152
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535866
ClinVar RCV Id: RCV000644078 RCV001014102 RCV000765268 RCV004003988
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala675Ser
CA276737715
NM_021055.3:c.2023G>T