Canonical Allele Identifier: PA2828053034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys356Asn
CA10584241
NM_001354905.2:c.1068G>C
CA16024690
NM_001354905.2:c.1068G>T