Canonical Allele Identifier: PA913200402
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2319Lys
CA16036502
NM_001127510.3:c.6956G>A