Canonical Allele Identifier: PA2827966962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1139Val
CA16028993
NM_001354898.2:c.3415A>G