Canonical Allele Identifier: PA2828412500
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406081
ClinVar RCV Id: RCV000475520 RCV000492042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala822Val
CA16614739
NM_001370404.1:c.2465C>T