Canonical Allele Identifier: PA2828016565
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg370Gly
CA16025594
NM_001354906.2:c.1108A>G