Allele Registry

Canonical Allele Identifier: PA103765

Gene: INSL3 HGNC NCBI

ClinVar Allele:

29870

ClinVar RCV:

RCV000015956

ClinVar Variation:

14831

HGVS (amino-acid)	Matching Registered Transcripts
NP_005534.2:p.Arg102Cys	CA210730 NM_005543.4:c.304C>T