Canonical Allele Identifier: PA915990063
Gene: VARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 488636
ClinVar RCV Id: RCV000578261 RCV000622841 RCV003431132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161205.1:p.Arg31Trp
CA3705627
NM_001167733.3:c.91C>T