Canonical Allele Identifier: PA2827986911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1641Ser
CA16032360
NM_001354900.2:c.4921G>A