Canonical Allele Identifier: PA2827976638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu1289Gln
CA008815
NM_001354899.2:c.3865G>C