Canonical Allele Identifier: PA194666
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn2810Ser
CA015484
NM_000038.6:c.8429A>G