Canonical Allele Identifier: PA2827976134
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1136Val
CA16028993
NM_001354899.2:c.3406A>G