Canonical Allele Identifier: PA2828019071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 923028
ClinVar RCV Id: RCV001183414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly756Ala
CA16028162
NM_001354906.2:c.2267G>C