Canonical Allele Identifier: PA2825021183
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser1658Thr
CA16032217
NM_000038.6:c.4973G>C