Canonical Allele Identifier: PA2826989952
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 411193
ClinVar RCV Id: RCV000595240 RCV001088024 RCV001166927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305310.1:p.Asn552Ser
CA5158513
NM_001318381.2:c.1655A>G