Canonical Allele Identifier: PA2827987110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys1698Arg
CA009933
NM_001354900.2:c.5093A>G