ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825437377
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
141482
ClinVar RCV Id:
RCV000130032
RCV001087672
RCV000836828
RCV003997543
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001070651.1:p.Ala1064Val
CA018885
NM_001077183.3:c.3191C>T