Canonical Allele Identifier: PA2827975462
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser942Asn
CA033901
NM_001354899.2:c.2825G>A