Canonical Allele Identifier: PA645385121
Gene: LIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329978
ClinVar RCV Id: RCV000385729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085915.2:p.Val14Met
CA9611645
NM_030657.4:c.40G>A