Canonical Allele Identifier: PA1139750448
Gene: VSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 885150
ClinVar RCV Id: RCV001116574 RCV001116575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878314.1:p.Ala217Pro
CA390369275
NM_182894.3:c.649G>C