Canonical Allele Identifier: PA2828007340
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser879Asn
CA033901
NM_001354902.2:c.2636G>A