Canonical Allele Identifier: PA2499252149
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1019045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2696Asp
CA16038773
NM_001354896.2:c.8086A>G