Allele Registry

Canonical Allele Identifier: PA2825644658

Gene: APC HGNC NCBI

ClinVar Variation Id: 470111

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Gln2587His	CA16038310 NM_001127511.3:c.7761A>C CA16038311 NM_001127511.3:c.7761A>T