Canonical Allele Identifier: PA2827962742
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2669Leu
CA16038652
NM_001354897.2:c.8005G>C
CA16038653
NM_001354897.2:c.8005G>T