Canonical Allele Identifier: PA2827978108
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587040
ClinVar RCV Id: RCV003339117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1732Ala
CA16032867
NM_001354899.2:c.5194C>G