Canonical Allele Identifier: PA645470051
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 289200
ClinVar RCV Id: RCV000310454 RCV001859698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.Leu945His
CA5158723
NM_014425.5:c.2834T>A