Canonical Allele Identifier: PA286695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2754Asn
CA014491
NM_000038.6:c.8261G>A