Allele Registry

Canonical Allele Identifier: PA109016

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000010391

ClinVar Variation:

9738

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Phe109Ser	CA254865 NM_003140.3:c.326T>C