Canonical Allele Identifier: PA916022937
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536104
ClinVar RCV Id: RCV001026437 RCV000644409 RCV003328614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asn48Ser
CA056283
NM_001318831.2:c.143A>G