Canonical Allele Identifier: PA2827949086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu140Asp
CA008951
NM_001354896.2:c.420G>C
CA16022242
NM_001354896.2:c.420G>T