Canonical Allele Identifier: PA2828052079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His248Gln
CA16023326
NM_001354905.2:c.744T>A
CA16023327
NM_001354905.2:c.744T>G