Canonical Allele Identifier: PA2827979149
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2055Met
CA011046
NM_001354899.2:c.6165A>G