Canonical Allele Identifier: PA916041912
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu432Lys
CA026951
NM_001354897.2:c.1294G>A