Canonical Allele Identifier: PA2827996255
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1702Ser
CA041233
NM_001354901.2:c.5105A>G