Canonical Allele Identifier: PA915990110
Gene: VARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 488637
ClinVar RCV Id: RCV000578459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161206.1:p.Arg497Pro
CA363173169
NM_001167734.2:c.1490G>C