Allele Registry

Canonical Allele Identifier: PA103783

Gene: INSL3 HGNC NCBI

ClinVar Allele:

29869

ClinVar RCV:

RCV000015955

ClinVar Variation:

14830

HGVS (amino-acid)	Matching Registered Transcripts
NP_005534.2:p.Pro93Leu	CA210729 NM_005543.4:c.278C>T