Canonical Allele Identifier: PA2825018820
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 646667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1118Thr
CA035129
NM_000038.6:c.3353A>C