Canonical Allele Identifier: PA2827988546
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2144Asn
CA045325
NM_001354900.2:c.6431G>A