Canonical Allele Identifier: PA2828006558
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 993040
ClinVar RCV Id: RCV001283862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1375Ser
CA16031416
NM_001354905.2:c.4124A>G