Canonical Allele Identifier: PA2827940694
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys398Arg
CA026866
NM_001354895.2:c.1193A>G