Canonical Allele Identifier: PA2827973661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 802134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His364Gln
CA16023880
NM_001354899.2:c.1092C>A
CA16023881
NM_001354899.2:c.1092C>G