Canonical Allele Identifier: PA2825436125
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1425749
ClinVar RCV Id: RCV001926881 RCV004010909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro666Ser
CA394274426
NM_001077183.3:c.1996C>T