Allele Registry

Canonical Allele Identifier: PA2826484908

Gene: INSL3 HGNC NCBI

ClinVar RCV:

RCV001650727

RCV001730924

ClinVar Variation:

1253265

HGVS (amino-acid)	Matching Registered Transcripts
NP_001252516.1:p.Thr60Ala	CA9301295 NM_001265587.2:c.178A>G