Canonical Allele Identifier: PA2825014940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala440Thr
CA16024191
NM_000038.6:c.1318G>A