Allele Registry

Canonical Allele Identifier: PA2827954383

Gene: APC HGNC NCBI

ClinVar Variation Id: 1061069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341826.1:p.Ser52Arg	CA360612181 NM_001354897.2:c.154A>C CA360612194 NM_001354897.2:c.156C>A CA360612197 NM_001354897.2:c.156C>G