Allele Registry

Canonical Allele Identifier: PA108996

Gene: SRY HGNC NCBI

ClinVar Allele:

24786

ClinVar RCV:

RCV000010401

ClinVar Variation:

9747

HGVS (amino-acid)	Matching Registered Transcripts
NP_003131.1:p.Met64Ile	CA254875 NM_003140.3:c.192G>A CA414941586 NM_003140.3:c.192G>T CA414941587 NM_003140.3:c.192G>C