Canonical Allele Identifier: PA658686021
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg527Thr
CA16024760
NM_001127510.3:c.1580G>C