Canonical Allele Identifier: PA916040875
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2010Ala
CA16034411
NM_001354896.2:c.6028C>G