Canonical Allele Identifier: PA262936
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49812
ClinVar RCV Id: RCV000043078 RCV002326761 RCV001852896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val1407Leu
CA020086
NM_000548.5:c.4219G>C
CA394300056
NM_000548.5:c.4219G>T