Canonical Allele Identifier: PA2827964505
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 802134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.His367Gln
CA16023880
NM_001354898.2:c.1101C>A
CA16023881
NM_001354898.2:c.1101C>G