Allele Registry

Canonical Allele Identifier: PA916039728

Gene: APC HGNC NCBI

ClinVar RCV:

RCV003538435

RCV004025698

ClinVar Variation:

537436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341825.1:p.Trp717Cys	CA16025911 NM_001354896.2:c.2151G>C CA16025912 NM_001354896.2:c.2151G>T