Canonical Allele Identifier: PA916042163
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala229Thr
CA16022765
NM_001354902.2:c.685G>A