Canonical Allele Identifier: PA2825642089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys1753Arg
CA16032947
NM_001127511.3:c.5258A>G