Canonical Allele Identifier: PA2827940998
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp491Glu
CA16024530
NM_001354895.2:c.1473C>A
CA16024531
NM_001354895.2:c.1473C>G