Canonical Allele Identifier: PA916042459
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Glu81Asp
CA008951
NM_001354905.2:c.243G>C
CA16022242
NM_001354905.2:c.243G>T