Canonical Allele Identifier: PA2828024441
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1625Ser
CA16033859
NM_001354906.2:c.4874A>G