Canonical Allele Identifier: PA915990067
Gene: VARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 506357
ClinVar RCV Id: RCV000676483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161205.1:p.Gly63Arg
CA3705666
NM_001167733.3:c.187G>A
CA363168204
NM_001167733.3:c.187G>C