Canonical Allele Identifier: PA2828002460
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1466Asn
CA16031568
NM_001354902.2:c.4397T>A