Canonical Allele Identifier: PA2827994065
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1049Ser
CA035035
NM_001354901.2:c.3146A>G