Canonical Allele Identifier: PA2827978157
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692247
ClinVar RCV Id: RCV002257119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1747Leu
CA16032973
NM_001354899.2:c.5240C>T