Canonical Allele Identifier: PA2825915587
Gene: LIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329972
ClinVar RCV Id: RCV000359963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155220.1:p.Val112Ile
CA9611503
NM_001161748.2:c.334G>A