Allele Registry

Canonical Allele Identifier: PA114942

Gene: VANGL1 HGNC NCBI

ClinVar RCV:

RCV000001412

RCV000782228

ClinVar Variation:

1347

HGVS (amino-acid)	Matching Registered Transcripts
NP_620409.1:p.Arg274Gln	CA114941 NM_138959.3:c.821G>A