Canonical Allele Identifier: PA2827975958
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1090Ser
CA16028677
NM_001354899.2:c.3269A>G