Canonical Allele Identifier: PA2828023918
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587040
ClinVar RCV Id: RCV003339117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro1659Ala
CA16032867
NM_001354903.2:c.4975C>G