Canonical Allele Identifier: PA262791
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49595
ClinVar RCV Id: RCV000042856 RCV000336828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Phe897Ser
CA017895
NM_000548.5:c.2690T>C