Canonical Allele Identifier: PA2827984566
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser929Asn
CA033901
NM_001354900.2:c.2786G>A