ClinGen Allele Registry
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Canonical Allele Identifier:
PA916023664
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013205
RCV000042946
RCV000055317
RCV000414340
RCV000491426
RCV000768118
ClinVar Variation:
12397
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305761.1:p.Arg622Gln
CA015920
NM_001318832.2:c.1865G>A