Canonical Allele Identifier: PA2828414805
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238055
ClinVar RCV Id: RCV000233971 RCV003165608 RCV003463660 RCV003998830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile1501Val
CA10583336
NM_001370404.1:c.4501A>G