Canonical Allele Identifier: PA2828013405
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg2510Gly
CA16038727
NM_001354905.2:c.7528A>G