Canonical Allele Identifier: PA2827980592
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1722138
ClinVar RCV Id: RCV003743932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2490Lys
CA16037750
NM_001354899.2:c.7470T>A
CA16037751
NM_001354899.2:c.7470T>G