Canonical Allele Identifier: PA2827969689
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1967Ala
CA16034411
NM_001354898.2:c.5899C>G