Canonical Allele Identifier: PA2829449013
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 488174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003364.1:p.Met209Leu
CA5562829
NM_003373.4:c.625A>T
CA377268197
NM_003373.4:c.625A>C