Canonical Allele Identifier: PA916041026
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2167Pro
CA011185
NM_001354896.2:c.6500A>C