Canonical Allele Identifier: PA2827982951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro389Ala
CA027206
NM_001354900.2:c.1165C>G