Canonical Allele Identifier: PA2827980825
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2562Asn
CA16038210
NM_001354899.2:c.7686A>C
CA16038211
NM_001354899.2:c.7686A>T