Canonical Allele Identifier: PA658808935
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 496840
ClinVar RCV Id: RCV000594073 RCV000766037 RCV001242893 RCV003962658 RCV004024696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055240.2:p.Gln796Glu
CA5158616
NM_014425.5:c.2386C>G