Canonical Allele Identifier: PA2827000798
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238099
ClinVar RCV Id: RCV000226007 RCV001019379 RCV001770191 RCV003998846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro279Gln
CA056703
NM_001318827.2:c.836C>A