Canonical Allele Identifier: PA2827978139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1374809
ClinVar RCV Id: RCV003745371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1740Asn
CA16032926
NM_001354899.2:c.5220G>C
CA16032927
NM_001354899.2:c.5220G>T