Canonical Allele Identifier: PA2825018940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1138Gly
CA035284
NM_000038.6:c.3413A>G