Canonical Allele Identifier: PA2827941701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2779708
ClinVar RCV Id: RCV003745664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys738Glu
CA16026178
NM_001354895.2:c.2212A>G