Canonical Allele Identifier: PA2827965540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn716Ser
CA007300
NM_001354898.2:c.2147A>G