Canonical Allele Identifier: PA2828022321
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile1274Asn
CA16031568
NM_001354906.2:c.3821T>A