Canonical Allele Identifier: PA2825023963
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2367Ala
CA046911
NM_000038.6:c.7099A>G