Canonical Allele Identifier: PA2827993638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser911Asn
CA033901
NM_001354901.2:c.2732G>A