Allele Registry

Canonical Allele Identifier: PA2827956280

Gene: APC HGNC NCBI

ClinVar RCV:

RCV003538435

RCV004025698

ClinVar Variation:

537436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341826.1:p.Trp709Cys	CA16025911 NM_001354897.2:c.2127G>C CA16025912 NM_001354897.2:c.2127G>T