Canonical Allele Identifier: PA2825625390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg71His
CA030877
NM_001127510.3:c.212G>A