Canonical Allele Identifier: PA2827980117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2349Ser
CA012867
NM_001354899.2:c.7046A>G