Canonical Allele Identifier: PA2826049337
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_001161205.1:p.Ala456Asp
CA215017
NM_001167733.3:c.1367C>A