Allele Registry

Canonical Allele Identifier: PA2826989709

Gene: INVS HGNC NCBI

ClinVar RCV:

RCV000081631

RCV000473554

RCV001166401

RCV003221802

ClinVar Variation:

95599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305310.1:p.Ser146Leu	CA148643 NM_001318381.2:c.437C>T