Allele Registry

Canonical Allele Identifier: PA2499263375

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV001533005

ClinVar Variation:

1177296

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Ala66Pro	CA414941576 NM_003140.3:c.196G>C