Allele Registry

Canonical Allele Identifier: PA2828015970

Gene: APC HGNC NCBI

ClinVar RCV:

RCV003536633

ClinVar Variation:

2748653

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341835.1:p.Ser263Gly	CA16024881 NM_001354906.2:c.787A>G CA2697546184 NM_001354906.2:c.786_787delinsAG