Canonical Allele Identifier: PA2827972206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2729Asn
CA014491
NM_001354898.2:c.8186G>A