Allele Registry

Canonical Allele Identifier: PA2741901149

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV003236645

ClinVar Variation:

2506477

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Thr102Ile	CA414941324 NM_003140.3:c.305C>T