Canonical Allele Identifier: PA2827950808
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1043Val
CA008024
NM_001354896.2:c.3127A>G