Canonical Allele Identifier: PA2827985212
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1123Val
CA16028993
NM_001354900.2:c.3367A>G