Canonical Allele Identifier: PA2825641799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1664Ser
CA16032360
NM_001127511.3:c.4990G>A