Canonical Allele Identifier: PA2827964589
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu397Lys
CA026951
NM_001354898.2:c.1189G>A