Allele Registry

Canonical Allele Identifier: PA2827975921

Gene: APC HGNC NCBI

ClinVar Variation Id: 411388

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Ala1079Ser	CA16028614 NM_001354899.2:c.3235G>T