Allele Registry

Canonical Allele Identifier: PA136763

Gene: VCL HGNC NCBI

ClinVar RCV:

RCV000038819

RCV000171847

RCV000619949

RCV000678764

RCV000727177

RCV000988386

RCV003227625

ClinVar Variation:

45602

HGVS (amino-acid)	Matching Registered Transcripts
NP_054706.1:p.Leu955del	CA136761 NM_014000.2:c.2862_2864del