Canonical Allele Identifier: PA2827997293
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2024Met
CA011046
NM_001354901.2:c.6072A>G