Canonical Allele Identifier: PA2828032937
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys390Asn
CA10584241
NM_001354904.2:c.1170G>C
CA16024690
NM_001354904.2:c.1170G>T