Canonical Allele Identifier: PA2827971946
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1019045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2653Asp
CA16038773
NM_001354898.2:c.7957A>G