Canonical Allele Identifier: PA2828001465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His963Pro
CA034499
NM_001354902.2:c.2888A>C