Allele Registry

Canonical Allele Identifier: PA108956

Gene: SRY HGNC NCBI

ClinVar Allele:

24780

ClinVar RCV:

RCV000010394

RCV000010395

ClinVar Variation:

9741

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Ile90Met	CA210695 NM_003140.3:c.270C>G