Canonical Allele Identifier: PA2825437199
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452351
ClinVar RCV Id: RCV000521882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr1015Ser
CA394285482
NM_001077183.3:c.3043A>T
CA394285499
NM_001077183.3:c.3044C>G