Canonical Allele Identifier: PA915988590
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 662766
ClinVar RCV Id: RCV000820493 RCV002537473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg1482Trp
CA2393787
NM_002292.4:c.4444C>T