Canonical Allele Identifier: PA2828012706
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro2589Ala
CA014255
NM_001354902.2:c.7765C>G