Allele Registry

Canonical Allele Identifier: PA109060

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000010408

ClinVar Variation:

9754

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Ser18Asn	CA254886 NM_003140.3:c.53G>A