Allele Registry

Canonical Allele Identifier: PA2825638783

Gene: APC HGNC NCBI

ClinVar RCV:

RCV003538435

RCV004025698

ClinVar Variation:

537436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120983.2:p.Trp681Cys	CA16025911 NM_001127511.3:c.2043G>C CA16025912 NM_001127511.3:c.2043G>T