Canonical Allele Identifier: PA658659763
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His1210Leu
CA035977
NM_001127510.3:c.3629A>T