Canonical Allele Identifier: PA2826990399
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 411193
ClinVar RCV Id: RCV000595240 RCV001088024 RCV001166927
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.Asn322Ser
CA5158513
NM_001318382.2:c.965A>G