Canonical Allele Identifier: PA2827957328
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1035Val
CA008024
NM_001354897.2:c.3103A>G