Canonical Allele Identifier: PA916042247
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr291Ala
CA050760
NM_001354902.2:c.871A>G