Allele Registry

Canonical Allele Identifier: PA094800

Gene: INVS HGNC NCBI

ClinVar RCV:

RCV000012738

RCV002512990

ClinVar Variation:

11960

HGVS (amino-acid)	Matching Registered Transcripts
NP_055240.2:p.Leu493Ser	CA121810 NM_014425.5:c.1478T>C