Allele Registry

Canonical Allele Identifier: PA2827982017

Gene: APC HGNC NCBI

ClinVar RCV:

RCV002341619

RCV003744802

ClinVar Variation:

1010973

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341829.1:p.Trp98Cys	CA16022352 NM_001354900.2:c.294G>C CA16022353 NM_001354900.2:c.294G>T