Canonical Allele Identifier: PA2827995926
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 651065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1606Ala
CA16032259
NM_001354901.2:c.4816C>G