Allele Registry

Canonical Allele Identifier: PA2826989949

Gene: INVS HGNC NCBI

ClinVar Variation Id: 194250

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305310.1:p.Lys546Arg	CA240125 NM_001318381.2:c.1637A>G