Canonical Allele Identifier: PA112859
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 7816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000305.3:p.His123Arg
CA000418
NM_000314.7:c.368A>G
CA891837402
NM_000314.7:c.367_369delinsAGA