Canonical Allele Identifier: PA262702
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49486
ClinVar RCV Id: RCV000042746 RCV001232925
ClinVar Variation Id: 65278
ClinVar RCV Id: RCV000055499 RCV004537245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gln1554His
CA020854
NM_000548.5:c.4662G>C
CA020857
NM_000548.5:c.4662G>T