Canonical Allele Identifier: PA658805114
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535888
ClinVar RCV Id: RCV000644107 RCV001568107 RCV002343304 RCV004003995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1766Leu
CA276759930
NM_000548.5:c.5297C>T