Canonical Allele Identifier: PA915959108
Gene: LINS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 129483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035706.2:p.Thr375Ile
CA231233
NM_001040616.3:c.1124C>T