ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645436513
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
238085
ClinVar RCV Id:
RCV000520770
RCV001086979
RCV002347871
RCV003998839
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000539.2:p.Pro1781Leu
CA10583347
NM_000548.5:c.5342C>T