Canonical Allele Identifier: PA916023632
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49173
ClinVar RCV Id: RCV000042429 RCV001298722 RCV001565367
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.His604Arg
CA015696
NM_001318832.2:c.1811A>G