Canonical Allele Identifier: PA2580276691
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081703
ClinVar RCV Id: RCV002995548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg1365Trp
CA2393875
NM_002292.4:c.4093C>T