Canonical Allele Identifier: PA2828008635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1748Ser
CA16033859
NM_001354905.2:c.5243A>G