Canonical Allele Identifier: PA2825915562
Gene: LIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329978
ClinVar RCV Id: RCV000385729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155220.1:p.Val14Met
CA9611645
NM_001161748.2:c.40G>A