Canonical Allele Identifier: PA353462
Gene: LIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224327
ClinVar RCV Id: RCV000209996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085915.2:p.Gly196Glu
CA353461
NM_030657.4:c.587G>A