Canonical Allele Identifier: PA2828000463
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg436Thr
CA16024760
NM_001354902.2:c.1307G>C