Allele Registry

Canonical Allele Identifier: PA279269

Gene: VCL HGNC NCBI

ClinVar RCV:

RCV000201438

ClinVar Variation:

217497

HGVS (amino-acid)	Matching Registered Transcripts
NP_054706.1:p.Asp511Tyr	CA279267 NM_014000.2:c.1531G>T