ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827002059
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000644078
RCV000765268
RCV001014102
RCV004003988
ClinVar Variation:
535866
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305756.1:p.Ala638Ser
CA276737715
NM_001318827.2:c.1912G>T