ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827000778
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000229314
RCV002372262
RCV003237787
RCV003998845
ClinVar Variation:
238097
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305756.1:p.Tyr273Cys
CA10583288
NM_001318827.2:c.818A>G