Canonical Allele Identifier: PA2827984906
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1040Asn
CA349100
NM_001354900.2:c.3119G>A