Canonical Allele Identifier: PA215018
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_001161206.1:p.Ala626Asp
CA215017
NM_001167734.2:c.1877C>A