Canonical Allele Identifier: PA2828042969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230729
ClinVar RCV Id: RCV004522844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1652His
CA16032990
NM_001354904.2:c.4955C>A