Canonical Allele Identifier: PA658675869
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472487
ClinVar RCV Id: RCV000544140 RCV004553240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg156His
CA352751228
NM_002292.4:c.467G>A