Canonical Allele Identifier: PA2827964525
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys373Arg
CA026866
NM_001354898.2:c.1118A>G