Canonical Allele Identifier: PA2825023691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2296Asn
CA16036358
NM_000038.6:c.6887G>A