Canonical Allele Identifier: PA645432304
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 384076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro677Leu
CA035873
NM_000548.5:c.2030C>T