Canonical Allele Identifier: PA2573205998
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn998Ser
CA16028071
NM_001354899.2:c.2993A>G