Canonical Allele Identifier: PA156852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg1640Gln
CA009812
NM_000038.6:c.4919G>A