Canonical Allele Identifier: PA2827977762
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1630Thr
CA16032217
NM_001354899.2:c.4889G>C