Canonical Allele Identifier: PA2827968972
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys1746Arg
CA16032947
NM_001354898.2:c.5237A>G