Canonical Allele Identifier: PA2827994276
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile1105Val
CA16028993
NM_001354901.2:c.3313A>G