Canonical Allele Identifier: PA2828007946
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1619Met
CA041612
NM_001354905.2:c.4857A>G