Canonical Allele Identifier: PA2828024797
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1807Ser
CA16033859
NM_001354903.2:c.5420A>G