Canonical Allele Identifier: PA2827956115
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly647Arg
CA16025491
NM_001354897.2:c.1939G>A
CA16025492
NM_001354897.2:c.1939G>C