Canonical Allele Identifier: PA2825181357
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232082
ClinVar RCV Id: RCV004518797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser526Arg
CA394326663
NM_000548.5:c.1576A>C
CA394326680
NM_000548.5:c.1578C>A
CA394326682
NM_000548.5:c.1578C>G