Canonical Allele Identifier: PA658673998
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 488174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Met209Leu
CA5562829
NM_014000.2:c.625A>T
CA377268197
NM_014000.2:c.625A>C