Canonical Allele Identifier: PA2829449970
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 487627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003364.1:p.Thr643Met
CA5563121
NM_003373.4:c.1928C>T