Allele Registry

Canonical Allele Identifier: PA2827979569

Gene: APC HGNC NCBI

ClinVar RCV:

RCV000130211

RCV000409211

RCV000484737

RCV000765788

RCV001157265

RCV002222403

RCV003650393

ClinVar Variation:

141618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341828.1:p.Met2185Ile	CA012330 NM_001354899.2:c.6555G>A CA16035852 NM_001354899.2:c.6555G>C CA16035853 NM_001354899.2:c.6555G>T