Canonical Allele Identifier: PA136729
Gene: VCL HGNC NCBI

Linked Data

ClinVar Variation Id: 45591
ClinVar RCV Id: RCV000038807 RCV000172505 RCV000769113 RCV003624402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054706.1:p.Ser600Arg
CA136727
NM_014000.2:c.1798A>C
CA377276650
NM_014000.2:c.1800C>G
CA377276652
NM_014000.2:c.1800C>A