Allele Registry

Canonical Allele Identifier: PA136801

Gene: VCL HGNC NCBI

ClinVar RCV:

RCV000038835

RCV000154123

RCV000252580

RCV000852615

RCV001084501

RCV003952439

ClinVar Variation:

45617

HGVS (amino-acid)	Matching Registered Transcripts
NP_054706.1:p.Thr197Ile	CA136799 NM_014000.2:c.590C>T