Canonical Allele Identifier: PA2825017206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly877Ala
CA032861
NM_000038.6:c.2630G>C