Allele Registry

Canonical Allele Identifier: PA2827991096

Gene: APC HGNC NCBI

ClinVar RCV:

RCV002341619

RCV003744802

ClinVar Variation:

1010973

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341830.1:p.Trp98Cys	CA16022352 NM_001354901.2:c.294G>C CA16022353 NM_001354901.2:c.294G>T