Canonical Allele Identifier: PA2828011648
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Lys2272Arg
CA012825
NM_001354902.2:c.6815A>G