Canonical Allele Identifier: PA2827977732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1620His
CA16032155
NM_001354899.2:c.4859C>A