Allele Registry

Canonical Allele Identifier: PA109090

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000541250

ClinVar Variation:

470196

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Tyr127Cys	CA414941142 NM_003140.3:c.380A>G