Allele Registry

Canonical Allele Identifier: PA2826990299

Gene: INVS HGNC NCBI

ClinVar RCV:

RCV000012738

RCV002512990

ClinVar Variation:

11960

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305311.1:p.Leu167Ser	CA121810 NM_001318382.2:c.500T>C