Allele Registry

Canonical Allele Identifier: PA2826484912

Gene: INSL3 HGNC NCBI

ClinVar Allele:

29869

ClinVar RCV:

RCV000015955

ClinVar Variation:

14830

HGVS (amino-acid)	Matching Registered Transcripts
NP_001252516.1:p.Pro125Ser	CA210729 NM_001265587.2:c.373C>T