Canonical Allele Identifier: PA645400206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1691Leu
CA16032423
NM_001127510.3:c.5072C>T