Canonical Allele Identifier: PA2827995509
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2444634
ClinVar RCV Id: RCV003154402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly1475Arg
CA16031406
NM_001354901.2:c.4423G>A
CA16031407
NM_001354901.2:c.4423G>C