Canonical Allele Identifier: PA2829191997
Gene: VIT HGNC NCBI

Linked Data

ClinVar Variation Id: 92022
ClinVar RCV Id: RCV000122579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001378898.1:p.Gly258Val
CA232368
NM_001391969.1:c.773G>T