Canonical Allele Identifier: PA658680314
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486635
ClinVar RCV Id: RCV000574722 RCV000644193 RCV004001156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Trp167Arg
CA394309129
NM_000548.5:c.499T>A
CA394309132
NM_000548.5:c.499T>C