Allele Registry

Canonical Allele Identifier: PA108884

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000010406

ClinVar Variation:

9752

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Arg133Trp	CA254883 NM_003140.3:c.397C>T