ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827005151
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
238071
ClinVar RCV Id:
RCV000228578
RCV000761036
RCV001023346
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305756.1:p.Phe1554Tyr
CA10583340
NM_001318827.2:c.4661T>A