Canonical Allele Identifier: PA2828001599
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181771
ClinVar Variation Id: 1730863
ClinVar RCV Id: RCV002451872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu1038Phe
CA008358
NM_001354902.2:c.3114G>T
CA16028752
NM_001354902.2:c.3114G>C