Canonical Allele Identifier: PA2828415930
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207654
ClinVar RCV Id: RCV000189880 RCV000475609 RCV001009700 RCV003996860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Lys34Thr
CA027975
NM_001370405.1:c.101A>C