Canonical Allele Identifier: PA2825637501
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His232Arg
CA16022971
NM_001127511.3:c.695A>G