Canonical Allele Identifier: PA103765
Gene: INSL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14831
ClinVar RCV Id: RCV000015956
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Amino-acid Alleles

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