Canonical Allele Identifier: PA2827998967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys2531Asn
CA16038210
NM_001354901.2:c.7593A>C
CA16038211
NM_001354901.2:c.7593A>T