Canonical Allele Identifier: PA916041886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys408Arg
CA026866
NM_001354897.2:c.1223A>G