Canonical Allele Identifier: PA658691645
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala219Thr
CA16022765
NM_001127510.3:c.655G>A