Canonical Allele Identifier: PA645485352
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 346012
ClinVar RCV Id: RCV000305973 RCV000360815 RCV000649516 RCV003480613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Glu85Lys
CA2394979
NM_002292.4:c.253G>A