Canonical Allele Identifier: PA2827982473
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser237Asn
CA16023257
NM_001354900.2:c.710G>A