ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827015476
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000470481
RCV000517116
RCV000562149
RCV004000719
ClinVar Variation:
406105
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305760.1:p.Ala1242Val
CA051222
NM_001318831.2:c.3725C>T