Canonical Allele Identifier: PA2828001693
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1073Val
CA16028993
NM_001354902.2:c.3217A>G