Canonical Allele Identifier: PA658681384
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1771Ala
CA055040
NM_000548.5:c.5311C>G