Canonical Allele Identifier: PA2828018990
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn743Ser
CA16028071
NM_001354906.2:c.2228A>G