Canonical Allele Identifier: PA915959107
Gene: LINS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 589349
ClinVar RCV Id: RCV002462099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035706.2:p.Ile374Thr
CA7759531
NM_001040616.3:c.1121T>C