Canonical Allele Identifier: PA2827998869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009233
ClinVar RCV Id: RCV003770591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu2499Phe
CA16037997
NM_001354901.2:c.7495C>T