Canonical Allele Identifier: PA2829449580
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003364.1:p.Ile519Leu
CA136703
NM_003373.4:c.1555A>C