Canonical Allele Identifier: PA2828011602
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2261Asn
CA16036703
NM_001354902.2:c.6782G>A