Canonical Allele Identifier: PA2828416387
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 834477
ClinVar RCV Id: RCV001035170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Val170Ala
CA394309232
NM_001370405.1:c.509T>C