Canonical Allele Identifier: PA286623
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1673Lys
CA009832
NM_001127510.3:c.5017G>A