Canonical Allele Identifier: PA645433844
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1358Ala
CA10583332
NM_000548.5:c.4072C>G