Canonical Allele Identifier: PA2828007739
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2158192
ClinVar RCV Id: RCV003653654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1049Leu
CA16028830
NM_001354902.2:c.3146C>T