Canonical Allele Identifier: PA2827993825
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn967Thr
CA16028070
NM_001354901.2:c.2900A>C