Allele Registry

Canonical Allele Identifier: PA108943

Gene: SRY HGNC NCBI

ClinVar RCV:

RCV000010400

ClinVar Variation:

9746

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Ile68Thr	CA254874 NM_003140.3:c.203T>C