Canonical Allele Identifier: PA2827945236
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn1798Asp
CA010373
NM_001354895.2:c.5392A>G