Canonical Allele Identifier: PA2827959598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly1713Arg
CA16032494
NM_001354897.2:c.5137G>A
CA16032495
NM_001354897.2:c.5137G>C