Allele Registry

Canonical Allele Identifier: PA109130

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000010392

RCV002460889

ClinVar Variation:

9739

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Val60Leu	CA254866 NM_003140.3:c.178G>C CA414941616 NM_003140.3:c.178G>T