Canonical Allele Identifier: PA2827960298
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1928Val
CA042868
NM_001354897.2:c.5782A>G