Canonical Allele Identifier: PA2827988228
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2042Met
CA011046
NM_001354900.2:c.6126A>G