Canonical Allele Identifier: PA2827959451
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1668Thr
CA16032217
NM_001354897.2:c.5003G>C