Canonical Allele Identifier: PA2827010405
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1622Ala
CA394314331
NM_001318829.2:c.4864C>G