Canonical Allele Identifier: PA2827943810
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gln1367Arg
CA16030311
NM_001354895.2:c.4100A>G