Allele Registry

Canonical Allele Identifier: PA913200302

Gene: APC HGNC NCBI

ClinVar Variation Id: 627841

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120982.1:p.Met1732Leu	CA16032681 NM_001127510.3:c.5194A>C CA16032682 NM_001127510.3:c.5194A>T