Allele Registry

Canonical Allele Identifier: PA658745033

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000581278

ClinVar Variation:

492908

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Arg30Ile	CA414941829 NM_003140.3:c.89G>T