Canonical Allele Identifier: PA165404
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2797Gly
CA015444
NM_000038.6:c.8389A>G