Canonical Allele Identifier: PA2827962514
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2600Asn
CA16038210
NM_001354897.2:c.7800A>C
CA16038211
NM_001354897.2:c.7800A>T