Allele Registry

Canonical Allele Identifier: PA2827970635

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000569441

RCV003537179

ClinVar Variation:

485093

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341827.1:p.Pro2259Leu	CA16036289 NM_001354898.2:c.6776C>T