Canonical Allele Identifier: PA286680
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu2603Gly
CA014080
NM_000038.6:c.7808A>G