Allele Registry

Canonical Allele Identifier: PA645391535

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000445559

ClinVar Variation:

393470

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Arg76Leu	CA16609283 NM_003140.3:c.227G>T