Allele Registry

Canonical Allele Identifier: PA108974

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000010396

ClinVar Variation:

9742

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Lys106Ile	CA254869 NM_003140.3:c.317A>T