Canonical Allele Identifier: PA2827998251
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln2316His
CA16036850
NM_001354901.2:c.6948A>C
CA16036851
NM_001354901.2:c.6948A>T