Canonical Allele Identifier: PA2826990458
Gene: INVS HGNC NCBI

Linked Data

ClinVar Variation Id: 289548
ClinVar RCV Id: RCV000393475 RCV000638082 RCV002502150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305311.1:p.Arg408Trp
CA5158579
NM_001318382.2:c.1222C>T