Canonical Allele Identifier: PA2828013442
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1019045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2518Asp
CA16038773
NM_001354905.2:c.7552A>G