Canonical Allele Identifier: PA189984
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2525His
CA013862
NM_000038.6:c.7574G>A