Allele Registry

Canonical Allele Identifier: PA2825015557

Gene: APC HGNC NCBI

ClinVar RCV:

RCV003536633

ClinVar Variation:

2748653

HGVS (amino-acid)	Matching Registered Transcripts
NP_000029.2:p.Ser546Gly	CA16024881 NM_000038.6:c.1636A>G CA2697546184 NM_000038.6:c.1635_1636delinsAG