Canonical Allele Identifier: PA2827977934
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1682Val
CA16032537
NM_001354899.2:c.5044A>G