Canonical Allele Identifier: PA2827957706
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2852532
ClinVar RCV Id: RCV003743093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1143Gly
CA16028780
NM_001354897.2:c.3428A>G