Canonical Allele Identifier: PA2827944974
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629228
ClinVar RCV Id: RCV000773927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly1721Val
CA16032616
NM_001354895.2:c.5162G>T