Canonical Allele Identifier: PA105592
Gene: VARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141426
ClinVar RCV Id: RCV000129935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065175.4:p.Ala596Asp
CA215017
NM_020442.5:c.1787C>A