Canonical Allele Identifier: PA2827968779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1691Ser
CA040767
NM_001354898.2:c.5072A>G