Canonical Allele Identifier: PA2828009636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1923Met
CA011046
NM_001354905.2:c.5769A>G