Canonical Allele Identifier: PA2828025617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile1800Met
CA011046
NM_001354906.2:c.5400A>G