Canonical Allele Identifier: PA2827968965
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1374809
ClinVar RCV Id: RCV003745371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys1743Asn
CA16032926
NM_001354898.2:c.5229G>C
CA16032927
NM_001354898.2:c.5229G>T