Canonical Allele Identifier: PA2827948121
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1019045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn2678Asp
CA16038773
NM_001354895.2:c.8032A>G