Canonical Allele Identifier: PA2828001386
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042543
ClinVar RCV Id: RCV002242366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp927Tyr
CA16028017
NM_001354902.2:c.2779G>T