Canonical Allele Identifier: PA2828095350
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro1671Ala
CA394314331
NM_001363528.2:c.5011C>G