Canonical Allele Identifier: PA645485406
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345996
ClinVar RCV Id: RCV000365545 RCV000392703 RCV002480206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg937Gln
CA2394201
NM_002292.4:c.2810G>A