Canonical Allele Identifier: PA2826990056
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_001305310.1:p.Gln700Glu
CA5158616
NM_001318381.2:c.2098C>G