Canonical Allele Identifier: PA2825015922
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 421285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr626Ala
CA029787
NM_000038.6:c.1876A>G