Allele Registry

Canonical Allele Identifier: PA2827980397

Gene: APC HGNC NCBI

ClinVar Variation Id: 1345335

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Phe2434Ser	CA16037417 NM_001354899.2:c.7301T>C