Canonical Allele Identifier: PA2826484914
Gene: INSL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14832
ClinVar RCV Id: RCV000015957 RCV002247347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001252516.1:p.Ala134Thr
CA210732
NM_001265587.2:c.400G>A